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PubMed (OMIM) for id: 5286
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Page 1
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction.
PLoS Genet. 2019 Apr 29;15(4):e1008088. doi: 10.1371/journal.pgen.1008088. eCollection 2019 Apr.
PLoS Genet. 2019.
PMID: 31034465
Free PMC article.
Spatiotemporal control of endocytosis by phosphatidylinositol-3,4-bisphosphate.
Posor Y, Eichhorn-Gruenig M, Puchkov D, Schöneberg J, Ullrich A, Lampe A, Müller R, Zarbakhsh S, Gulluni F, Hirsch E, Krauss M, Schultz C, Schmoranzer J, Noé F, Haucke V.
Posor Y, et al.
Nature. 2013 Jul 11;499(7457):233-7. doi: 10.1038/nature12360. Epub 2013 Jul 3.
Nature. 2013.
PMID: 23823722
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Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14.
Caldwell GM, Eddy RL, Day CD, Haley LH, Cooper PR, Sait SS, Hejtmancik F, Smith RJ, Morton CC, Higgins MJ, Shows TB.
Caldwell GM, et al.
Cytogenet Cell Genet. 2001;92(1-2):103-7. doi: 10.1159/000056877.
Cytogenet Cell Genet. 2001.
PMID: 11306805
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Cloning of a human phosphoinositide 3-kinase with a C2 domain that displays reduced sensitivity to the inhibitor wortmannin.
Domin J, Pages F, Volinia S, Rittenhouse SE, Zvelebil MJ, Stein RC, Waterfield MD.
Domin J, et al.
Biochem J. 1997 Aug 15;326 ( Pt 1)(Pt 1):139-47. doi: 10.1042/bj3260139.
Biochem J. 1997.
PMID: 9337861
Free PMC article.
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Cpk is a novel class of Drosophila PtdIns 3-kinase containing a C2 domain.
Molz L, Chen YW, Hirano M, Williams LT.
Molz L, et al.
J Biol Chem. 1996 Jun 7;271(23):13892-9. doi: 10.1074/jbc.271.23.13892.
J Biol Chem. 1996.
PMID: 8662856
Free article.
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